Aluminum chromate

Protactinium can be recovered from an aqueous nitrate solution of fission products and protactinium by adding sodium chromate, which brings down protactiniiun on the aluminum chromate precipitate. After dissolution of the precipitate in acid, protactinium may be recovered by solvent extraction, or it may be allowed to decay to which is more easily extracted [G4]. Protactinium can also be recovered by adsorption on powdered Vycor glass. 

Other compounds are of industrial value lead chromate is chrome yellow, a valued pigment. Chromium compounds are used in the textile industry as mordants, and by the aircraft and other industries for anodizing aluminum. 

Chromium Chromate. Chromium chromate treatment baths are acidic and made up from sources of hexavalent chromium and complex fluoride, fluorosiHcate, fluorozirconate, fluorotitanate, and siHcofluorides. Optional additional components added to accelerate coating rate are free fluoride, ferricyanide, and other metal salts such as barium nitrate. Conversion coating on aluminum precedes by the following reactions (2,3,17) ... 

Operation nd Control. Control of chromium chromate conversion coating baths is accompHshed by controlling chromium concentration and pH. The quaHty of the conversion coating is sensitive to aluminum accumulations in the coating bath as well as to rinse water purity. Sulfate contamination is a particular problem. 

Organochromium Catalysts. Several commercially important catalysts utilize organ ochromium compounds. Some of them are prepared by supporting bis(triphenylsilyl)chromate on siUca or siUca-alumina in a hydrocarbon slurry followed by a treatment with alkyl aluminum compounds (41). Other catalysts are based on bis(cyclopentadienyl)chromium deposited on siUca (42). The reactions between the hydroxyl groups in siUca and the chromium compounds leave various chromium species chemically linked to the siUca surface. The productivity of supported organochromium catalysts is also high, around 8—10 kg PE/g catalyst (800—1000 kg PE/g Cr). 

Sihcon carbide is comparatively stable. The only violent reaction occurs when SiC is heated with a mixture of potassium dichromate and lead chromate. Chemical reactions do, however, take place between sihcon carbide and a variety of compounds at relatively high temperatures. Sodium sihcate attacks SiC above 1300°C, and SiC reacts with calcium and magnesium oxides above 1000°C and with copper oxide at 800°C to form the metal sihcide. Sihcon carbide decomposes in fused alkahes such as potassium chromate or sodium chromate and in fused borax or cryohte, and reacts with carbon dioxide, hydrogen, ak, and steam. Sihcon carbide, resistant to chlorine below 700°C, reacts to form carbon and sihcon tetrachloride at high temperature. SiC dissociates in molten kon and the sihcon reacts with oxides present in the melt, a reaction of use in the metallurgy of kon and steel (qv). The dense, self-bonded type of SiC has good resistance to aluminum up to about 800°C, to bismuth and zinc at 600°C, and to tin up to 400°C a new sihcon nitride-bonded type exhibits improved resistance to cryohte. 

Modem manufacturing processes quench the roast by continuous discharge into the leach water held in tanks equipped with agitators. At this point the pH of the leach solution is adjusted to between 8 and 9 to precipitate aluminum and siHcon. The modem leaching operations are very rapid because no or htde lime is used. After separation of the ore residue and precipitated impurities using rotary vacuum filters, the cmde Hquid sodium chromate may need to be treated to remove vanadium, if present, in a separate operation. The ore residue and precipitants are either recycled or treated to reduce hexavalent chromium to Cr(III) before disposal. 

Aluminum. Eor aluminum alloys such as 1100 and 3003 only a cleaning operation is necessary before apphcation of enamel. Eor ahoy 6061, deoxidation and alkaline-chromate pretreatment processes may also be used to improve both the cleanliness of the surface and the development of enamel adherence. The spent chromium-containing solutions can present disposal problems and should be handled in accordance with existing regulations (19). 

Aluminum chlorate Ammonium chromate Benzoyl peroxide, dry... 

Chromate conversion coatings for aluminum are carried out in acidic solutions. These solutions usually contain one chromium salt, such as sodium chromate or chromic acid and a strong oxidizing agent such as hydrofluoric acid or nitric acid. The final film usually contains both products and reactants and water of hydration. Chromate films are formed by the chemical reaction of hexavalent chromium with a metal surface in the presence of accelerators such as cyanides, acetates, formates, sulfates, chlorides, fluorides, nitrates, phosphates, and sulfamates. 

Wastewaters from the coil coating on aluminum subcategory contain higher levels of cyanide and fluorides than the other subcategories as a result of chromating solutions containing cyanide ions... 

Lead(II) azide Lead chromate Lead dioxide Calcium stearate, copper, zinc, brass, carbon disulfide Iron hexacyanoferrate(4-) Aluminum carbide, hydrogen peroxide, hydrogen sulfide, hydroxylamine, ni-troalkanes, nitrogen compounds, nonmetal halides, peroxoformic acid, phosphorus, phosphorus trichloride, potassium, sulfur, sulfur dioxide, sulfides,... 

Many barium aluminosilicate-based compositions will eventually react with the chromium oxide or aluminum oxide scales on the metal interconnect or metal edge rails to form barium chromate or a celsian phase at the interface [6], This can cause a mechanical weakness that is easily delaminated. Also, compositions that contain boron can react over time with water (steam) to produce B2(OH)2 or B(OH)3 gas. This can decompose the glass and greatly limit the lifetime of the seal. Thus many of the new investigations have emphasized low or no boron glass compositions. 

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